EP0155852A2 - Substance liant la thrombine et procédé de préparation - Google Patents

Substance liant la thrombine et procédé de préparation Download PDF

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Publication number
EP0155852A2
EP0155852A2 EP85301959A EP85301959A EP0155852A2 EP 0155852 A2 EP0155852 A2 EP 0155852A2 EP 85301959 A EP85301959 A EP 85301959A EP 85301959 A EP85301959 A EP 85301959A EP 0155852 A2 EP0155852 A2 EP 0155852A2
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EP
European Patent Office
Prior art keywords
thrombin
binding substance
protein
affinity
substance
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP85301959A
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German (de)
English (en)
Other versions
EP0155852A3 (en
EP0155852B1 (fr
Inventor
Nobuo Aoki
Shinichiro Kurosawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kowa Co Ltd
Original Assignee
Kowa Co Ltd
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Publication date
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Application filed by Kowa Co Ltd filed Critical Kowa Co Ltd
Publication of EP0155852A2 publication Critical patent/EP0155852A2/fr
Publication of EP0155852A3 publication Critical patent/EP0155852A3/en
Application granted granted Critical
Publication of EP0155852B1 publication Critical patent/EP0155852B1/fr
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/745Blood coagulation or fibrinolysis factors
    • C07K14/7455Thrombomodulin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S530/00Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof
    • Y10S530/827Proteins from mammals or birds
    • Y10S530/85Reproductive organs or embryos
    • Y10S530/851Placenta; amniotic fluid

Definitions

  • This invention relates to a novel thrombin-binding substance and a process for producing such substance.
  • the present inventors have directed their extensive studies to the role of thrombin in the human coagulation and fibrinolysis mechanisms, especially to the effect of thrombin on the fibrinolysis mechanism. It has now been found that thrombin takes part in the activation of protein C even in human blood vessels and that a factor exists which, when bonded with thrombin, can accelerate the activation of protein C. It has also been found that this factor can be isolated in pure form from human placentae.
  • Another object of the invention is to provide a process for producing the thrombin-binding substance.
  • thrombin-binding substance derived from human tissue and having the following characteristics:
  • a thrombin-binding substance according to this invention can be produced, for example, by extracting fragments of a human placenta with a buffer containing a non-ionic surfactant, and then isolating the thrombin-binding substance in pure form from the resulting extract by means of diisopropylphosphoro-thrombin (hereinafter referred to simply as "DIP-thrombin'') affinity chromatography and/or gel filtration.
  • DIP-thrombin'' diisopropylphosphoro-thrombin
  • a human placenta is washed with a tris-HCl buffer containing sucrose and benzamidine hydrochloride, or with an analogous solution,and then ground into a homogeneous mixture.
  • the resulting mixture is centrifuged or similarly treated to collect a precipitate.
  • the precipitate is extracted with a solution which has been obtained by adding Triton X-100, Lubrol PX or the like to the buffer referred to above (Triton X-100 and Lubrol PX are trade names of products of Sigma Corporation).
  • the extract is caused to pass through a DIP-thrombin affinity chromatographic column packed with a carrier,such as DIP-thrombin-agarose,or the like to thereby allow active fractions to be adsorbed in the column.
  • a carrier such as DIP-thrombin-agarose,or the like.
  • gel filtration may be suitably employed to collect these active fractions.
  • affinity chromatography affinity chromatography
  • gel filtration techniques may be used in combination.
  • the thrombin-binding substance of the invention has the following characteristics.
  • the thrombin-binding substance of the invention promotes the thrombin-catalyzed activation of protein C.
  • the thrombin-binding substance of the invention has an anticoagulating effect on blood and hence prolongs the clotting time more as the concentration of the substance increases.
  • the substance of the invention (0.073 A 280/ ml) was treated at 25°C for 150 minutes under each of the conditions as listed above. After completion of the treatment, the resulting mixture was diluted 100 times with tris-buffered saline and measured with respect to its activity. From the activity level of an untreated sample, the residual activity was calculated. Pepsin was used in such an amount that the final concentration and pH reached 2.5 ⁇ g/ml and p H 2 .5, respectively. The pepsin treatment was performed at 37°C for 2 hours. The heat treatment was conducted at 100°C and at pH 7.5. The residual activity is expressed in terms of half time.
  • the precipitates collected were combined together and extracted with 300 ml of a 0.02 M tris-HC1 buffer (pH 7.5) containing 0.25 M sucrose, 1 mM of benzamidine hydrochloride and 0.5% (v/v) Triton X-100 to thereby obtain a crude extract.
  • the protein concentration of the crude extract (315 ml) was 1.17 A 280 /ml.
  • the crude extract (315 ml) was then subjected to a DIP-thrombin-agarose column which had been equilibrated with a 0.02 M tris-HC1 buffer (pH 7.5) containing 0.1 M sodium chloride, 0.5 mM calcium chloride, 0.1 mM benzamidine hydrochloride and 0.5% (v/v) Triton X-100.
  • the column was then washed with 1,500 ml of the buffer which had been used for the equilibration. The washings were collected in 16.7 ml-fractions by means of a fraction collector.
  • the column was then eluted using as an eluant 350 ml of a 0.02 M tris-HC1 buffer ( p H 7.5) containing 1 M of sodium chloride, 0.1 mM of EDT A , 1 mM of benzamidine hydrochloride and 0.5% (v/v) Triton X-100.
  • the protein concentrations and activity levels of the washings and eluate were respectively measured. The results are shown in FIG. 3.
  • the protein concentrations were measured in accordance with Lowry's method, while the activity levels were measured by the method set forth under Measurement Method 1 of paragraph (d) above.
  • the 38th to 57th eluate fractions were collectd to obtain 88 ml of the thrombin-binding substance of the invention, the protein concentration of which was 0.057 A 280 /ml.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Zoology (AREA)
  • Toxicology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Diabetes (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
EP85301959A 1984-03-23 1985-03-21 Substance liant la thrombine et procédé de préparation Expired - Lifetime EP0155852B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP59055792A JPS60199819A (ja) 1984-03-23 1984-03-23 トロンビン結合性物質およびその製法
JP55792/84 1984-03-23

Publications (3)

Publication Number Publication Date
EP0155852A2 true EP0155852A2 (fr) 1985-09-25
EP0155852A3 EP0155852A3 (en) 1988-03-23
EP0155852B1 EP0155852B1 (fr) 1990-05-02

Family

ID=13008759

Family Applications (1)

Application Number Title Priority Date Filing Date
EP85301959A Expired - Lifetime EP0155852B1 (fr) 1984-03-23 1985-03-21 Substance liant la thrombine et procédé de préparation

Country Status (4)

Country Link
US (1) US4638050A (fr)
EP (1) EP0155852B1 (fr)
JP (1) JPS60199819A (fr)
DE (1) DE3577399D1 (fr)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0239644A4 (fr) * 1985-06-28 1987-10-27 Asahi Chemical Ind Nouvelle substance physiologiquement active limitant la coagulation du sang.
EP0264060A3 (en) * 1986-10-14 1988-07-27 Kowa Company, Ltd. Anticoagulating substance and preparation process thereof
WO1988005659A1 (fr) * 1987-02-06 1988-08-11 Zymogenetics, Inc. Proteines humaines possedant une activite anticoagulante et anti-inflammatoire
EP0356836A3 (en) * 1988-08-29 1990-03-28 Kowa Company, Ltd. Thrombin-binding substance and process for preparing the same
EP0444441A3 (en) * 1990-03-01 1992-09-09 Hewlett-Packard Company Minimizing eluate band widths in liquid chromatography
US5516659A (en) * 1990-06-27 1996-05-14 Mochida Pharmaceutical Co., Ltd. Truncated thrombomodulin, recombinant production thereof, and therapeutic agent
US6034060A (en) * 1987-01-08 2000-03-07 Asahi Kasei Kogyo Kabushiki Kaisha Peptide having an ability to promote the activation of protein C by thrombin
WO2010138024A3 (fr) * 2009-05-29 2011-02-10 Общество С Ограниченной Ответственностью "Медицинский Исследовательский Центр "Иммункулус" Préparation pour la protection des cellules cérébrales

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4795804A (en) * 1983-08-16 1989-01-03 The Regents Of The University Of California Bone morphogenetic agents
DE3346953A1 (de) * 1983-12-24 1985-08-14 Organogen Medizinisch-Molekularbiologische Forschungsgesellschaft mbH, 6900 Heidelberg Cardiodilatin, ein neues peptidhormon und verfahren zu seiner herstellung
DK166587B1 (da) * 1984-09-21 1993-06-14 Boehringer Ingelheim Int Blodkoagulationshaemmende proteiner, fremgangsmaade til deres fremstilling samt deres anvendelse
JPH0689014B2 (ja) * 1986-01-21 1994-11-09 興和株式会社 トロンビン結合性物質およびその製法
JPS63146898A (ja) * 1986-07-15 1988-06-18 Kowa Co トロンビン結合性物質およびその製法
ATE113062T1 (de) * 1986-07-15 1994-11-15 Kowa Co Throminbindende substanz und verfahren zu ihrer herstellung.
JPH0798840B2 (ja) * 1988-12-27 1995-10-25 持田製薬株式会社 尿由来の抗血液疑固物質、その製法およびそれを含有する医薬組成物
US5202421A (en) * 1988-12-27 1993-04-13 Mochida Pharmaceutical Co., Ltd. Anticoagulant substance obtained from urine and process for the preparation thereof

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE636817A (fr) * 1962-08-31
BE787961A (fr) * 1971-08-24 1973-02-26 Behringwerke Ag Procede d'isolement d'une matiere thromboplastique et medicament contenant ladite matiere
DE2720704C2 (de) * 1977-05-07 1986-09-25 Behringwerke Ag, 3550 Marburg Neues Glycoprotein, Verfahren zu seiner Herstellung und seine Verwendung
DE2726886A1 (de) * 1977-06-15 1979-01-18 Behringwerke Ag Neues glykoprotein und verfahren zu dessen herstellung
DE2842467A1 (de) * 1978-09-29 1980-04-10 Behringwerke Ag Neues ubiquitaeres gewebsprotein pp tief 8
DE3038163A1 (de) * 1980-10-09 1982-05-06 Boehringer Mannheim Gmbh, 6800 Mannheim Thrombininhibitor, seine herstellung und verwendung

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0239644A4 (fr) * 1985-06-28 1987-10-27 Asahi Chemical Ind Nouvelle substance physiologiquement active limitant la coagulation du sang.
EP0264060A3 (en) * 1986-10-14 1988-07-27 Kowa Company, Ltd. Anticoagulating substance and preparation process thereof
US4873222A (en) * 1986-10-14 1989-10-10 Kowa Co, Ltd. Placenta-derived anticoagulating substance
US6034060A (en) * 1987-01-08 2000-03-07 Asahi Kasei Kogyo Kabushiki Kaisha Peptide having an ability to promote the activation of protein C by thrombin
WO1988005659A1 (fr) * 1987-02-06 1988-08-11 Zymogenetics, Inc. Proteines humaines possedant une activite anticoagulante et anti-inflammatoire
EP0356836A3 (en) * 1988-08-29 1990-03-28 Kowa Company, Ltd. Thrombin-binding substance and process for preparing the same
US5043425A (en) * 1988-08-29 1991-08-27 Kowa Co., Ltd. Thrombin-binding protein substance and process for preparing the same
EP0444441A3 (en) * 1990-03-01 1992-09-09 Hewlett-Packard Company Minimizing eluate band widths in liquid chromatography
US5516659A (en) * 1990-06-27 1996-05-14 Mochida Pharmaceutical Co., Ltd. Truncated thrombomodulin, recombinant production thereof, and therapeutic agent
US5695964A (en) * 1990-06-27 1997-12-09 Mochida Pharmaceutical Co., Ltd. Recombinant DNA vectors, including plasmids, and host cells for production of truncated thrombomodulin
WO2010138024A3 (fr) * 2009-05-29 2011-02-10 Общество С Ограниченной Ответственностью "Медицинский Исследовательский Центр "Иммункулус" Préparation pour la protection des cellules cérébrales

Also Published As

Publication number Publication date
EP0155852A3 (en) 1988-03-23
DE3577399D1 (de) 1990-06-07
EP0155852B1 (fr) 1990-05-02
JPS60199819A (ja) 1985-10-09
JPH0545600B2 (fr) 1993-07-09
US4638050A (en) 1987-01-20

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